Bromide

Bromide

SCHEMBL2449254

CCOc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.[Br-]

nearest known ligand 0.53

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

The experimentally established mechanism targets of Bromide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SNCA P37840 2/20 0.53
LTA4H P09960 1/20 0.52
MEN1 O00255 1/20 0.49
KMT2A Q03164 1/20 0.49
L3MBTL1 Q9Y468 1/20 0.49
NQO1 P15559 1/20 0.48
RELA Q04206 1/20 0.47
SIGMAR1 Q99720 1/20 0.47
RAB9A P51151 4/20 0.42
NPC1 O15118 3/20 0.42
CNR2 P34972 1/20 0.42
ACACB O00763 1/20 0.42
SMN1; SMN2 Q16637 3/20 0.41
HPGD P15428 2/20 0.41
LMNA P02545 1/20 0.41
KDM4E B2RXH2 1/20 0.41
ALDH1A1 P00352 1/20 0.41
TP53 P04637 1/20 0.41
TSHR P16473 1/20 0.41
TDP1 Q9NUW8 1/20 0.41

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Hydrochloric Acid SCHEMBL3156511 0.97 LTA4H (0.52) SNCALTA4HMEN1KMT2AL3MBTL1
Water SCHEMBL8527845 0.97 LTA4H (0.52) SNCALTA4HMEN1KMT2AL3MBTL1
Iodide SCHEMBL7909299 0.97 LTA4H (0.52) SNCALTA4HMEN1KMT2AL3MBTL1
SCHEMBL8372239 0.92 LTA4H (0.47) SNCALTA4HMEN1KMT2AL3MBTL1
SCHEMBL8375288 0.92 LTA4H (0.47) SNCALTA4HMEN1KMT2AL3MBTL1
Bromide SCHEMBL1044358 0.87 LTA4H (0.54) SNCALTA4HSMN1; SMN2LMNAALDH1A1
Bromide SCHEMBL28338224 0.86 CALM1 (0.43) SNCAMEN1KMT2ASIGMAR1SMN1; SMN2
Iodide SCHEMBL1047429 0.83 LTA4H (0.54) SNCALTA4H
Hydrochloric Acid SCHEMBL1046793 0.83 LTA4H (0.54) SNCALTA4H
SCHEMBL8375290 0.83 SNCA (0.42) SNCALTA4HMEN1KMT2AL3MBTL1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 120 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6248161-B1 Preparation of permanent color inks from water-soluble colorants using specific phosphonium salts HEWLETT-PACKARD COMPANY 2001-06-19 US claimed
US-6210816-B1 Translucent xerographic recording substrates XEROX CORPORATION 2001-04-03 US claimed
EP-0743574-B1 Migration imaging members XEROX CORP (US) 2000-12-27 EP claimed
EP-0743573-B1 Method for obtaining image contrast migration imaging members XEROX CORP (US) 2000-09-06 EP claimed
US-6086661-A (A)IMIDAZOLINIUM QUATERNARY SALT, (B) PHOSPHONIUM QUATERNARY SALT, OR (C) AN AMMONIUM QUATERNARY SALT; A PAPER-CURL REDUCING COMPOUND; DYE; STABILIZERS, BIOCIDE, WATER SOLUBLE SALT XEROX CORPORATION (US) 2000-07-11 US claimed
US-5760809-A INK JET PRINTING XEROX CORPORATION (US) 1998-06-02 US claimed
US-5665802-A REACTING POLYAMIC ACID WITH A DEHYDRATION-CYCLIZATION AGENT, A CATALYST AND AN ORGANIC PHOSPHORUS COMPOUND; EXCELLENT IN TENSILE STRENGTH AND FLEXIBILITY KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1997-09-09 US claimed
EP-0743573-A2 Method for obtaining image contrast migration imaging members XEROX CORPORATION (US) 1996-11-20 EP claimed
EP-0743574-A2 Migration imaging members XEROX CORPORATION (US) 1996-11-20 EP claimed
EP-0615853-B1 Recording sheets containing phosphonium compounds XEROX CORP (US) 1996-10-16 EP claimed
US-5563014-A SOFTENABLE LAYER CONTAINIG PHOTOSENSITIVE MARKING MATERIAL; TRANSPARENTIZING AGENT XEROX CORPORATION (US) 1996-10-08 US claimed
US-5514505-A SELECTIVE TRANSPARENTIZATION OF PHOTOSENSITIVE MIGRATION MARKING PARTICLES EMBEDDED NEAR THE SURFACE OF A SOFTENABLE LAYER SUPPORTED BY AN ELECTROCONDUCTIVE SUBSTRATE XEROX CORPORATION (US) 1996-05-07 US claimed
EP-0477472-B1 Process for the preparation of cyclic carbonates RUETGERSWERKE AG (DE) 1995-12-13 EP claimed
US-5153333-A Reacting epoxy compound with carbon dioxide in presence of quaternary phosphonium halide catalyst RUTGERSWERKE AG (DE) 1992-10-06 US claimed
WO-2026087965-A1 COMPOSITION COMPRISING EPOXY RESIN WITH CONSTRAINED AROMATIC RINGS AND PHOTOBASE 3M INNOVATIVE PROPERTIES COMPANY (US) 2026-04-30 WO disclosed
WO-2025200154-A1 TWO-PART EPOXY COMPOSITION COMPRISING THIOL CURATIVE, AND CATALYST 3M INNOVATIVE PROPERTIES COMPANY (US) 2025-10-02 WO disclosed
US-20240309240-A1 POLISHING COMPOSITION, POLISHING METHOD, AND METHOD FOR PRODUCING SEMICONDUCTOR SUBSTRATE FUJIMI INCORPORATED (JP) 2024-09-19 US disclosed
US-5153333-A Reacting epoxy compound with carbon dioxide in presence of quaternary phosphonium halide catalyst RUTGERSWERKE AG (DE) 1992-10-06 US disclosed
EP-0477472-A1 Process for the preparation of cyclic carbonates Bakelite AG (DE) 1992-04-01 EP disclosed
EP-0350958-A2 Improved polyimide and polyimide film and manufacturing method thereof KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1990-01-17 EP disclosed